Ganglioglioma

Ganglioglioma is a rare, usually benign, brain tumor that originates from nerve cells and is most commonly found in children and young adults. The tumor is composed of both neuronal (ganglionic) and glial (supportive) cells.

Symptoms

The symptoms of ganglioglioma can vary depending on the location of the tumor. Common symptoms include seizures, headaches, and neurological deficits such as weakness or numbness in the limbs or face.

Diagnosis

MRI and CT scans are typically used to diagnose ganglioglioma. A biopsy may also be performed to confirm the diagnosis and determine the grade of the tumor.

Treatment

Treatment for ganglioglioma usually involves surgery to remove as much of the tumor as possible. In some cases, radiation therapy or chemotherapy may be used if the tumor cannot be completely removed or if it recurs after surgery.

Prognosis

The prognosis for individuals with ganglioglioma is generally good, especially if the tumor can be completely removed. However, the tumor can recur, and in rare cases, it can transform into a malignant tumor.

See also

• Brain tumor
• Neurology
• Oncology

References

Ganglioglioma Resources
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